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  • 1
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Heterogeneous olefin polymerization catalysts generally consist of a transition metal compound from groups IVB or VB in combination with an organometallic compound from groups I, II, and III of the periodic table of the elements, but in some instances may contain a third component possessing at least one strongly complexing ligand atom. The composition of a coordination catalyst of this type determines both the rate of polymerization of the α-olefin and the stereoregularity of the polymer produced. In order to predict activity and stereospecificity of catalysts for the polymerization of α-olefins, data from the polymerization of propylene using catalysts of the following types were correlated: (1) titanium(III) chloride catalysts in which the organometallic component was varied, (2) coordination catalysts containinig a ligand third component in which the ligand was varied, and (3) coordination catalysts in which the transition metal component was varied.The electronegativity of an orgariometallic compound is known to be important in determining its reactivity with ethers, hydrogen, and other reagents. Both the ionic size and the electronegativity of the central atom appear to be important in determining the utility of both the organometallic and the transition metal compounds as components for coordination catalysts. In general, organometallic and transition metal compounds having small central atoms with similar electronegativities favor the formation of stereospecific catalysts.The present correlation has made it possible to predict the activity and stereospecificity of coordination catalysts for olefin polymerization.
    Additional Material: 11 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 58 (1962), S. 881-909 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Conversion of ethylene to a high-density polymer was readily effected at low pressures and temperatures with the use of a catalyst consisting initially of a mixture of aluminum and titanium(IV) chloride. The principal factors influencing the polymerization and properties of the resulting polyethylene were investigated. These reactions at preferred catalyst concentrations were always preceded by a prolonged induction period; consequently, a means of reducing this period was developed. Factors influencing the polymerization included the nature of the aluminum in the catalyst, type of solvent, and molecular weight regulators. The effects of pressure, temperature, aluminum concentration, and Al/TiCl4 mole ratio on induction period, reaction rate, and polymer properties were determined from a factorial experiment in which each factor was investigated at two levels. The polymerization could be initiated at low catalyst concentrations and temperatures by preactivating the Al-TiCl4 mixture, that is, partially converting it to aluminum chloride and titanium(III) chloride. Optimum catalyst efficiency was obtained at an Al/TiCl4 mole ratio of 0.5 to 1.0; the aluminum concentration was 0.0028 to 0.04% based on weight of solvent. Polyethylene yields as great as 1873 parts/part total catalyst were obtained at aluminum concentrations of 0.0028 to 0.008% and ethylene pressures of 150 to 280 psi. Liquid aliphatic hydrocarbons were more effective than aromatic hydrocarbons as media for the polymerization. Low molecular weight polymers and high-density waxes were produced when hydrogen was used in the polymerization. The statistical study showed that the induction period was reduced by increasing the ethylene pressure and by decreasing the Al/TiCl4 mole ratio. The average reaction rate was increased by increasing the pressure, temperature, and aluminum concentration. A kinetic analysis of the data showed that the length of the induction period was inversely proportional to the first power of the pressure and titanium(IV) chloride concentration. The rate equation for the polymerization was found to be \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm average rate = }B{\rm [TiCl}_{\rm 4} {\rm ][Al]}^{{\rm 1/2}} P^{1/2} e^{ - {{4100} \mathord{\left/ {\vphantom {{4100} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}}$$\end{document} where P is the ethylene pressure. Formation of high molecular weight polymers was favored by high monomer concentrations and low titanium(IV) chloride concentrations. High-density polyethylene (0.950-0.960 g./cc.) can be produced conveniently, safely, and economically at low pressures (40 to 280 psi) and low temperatures (50 to 85°C.) with the use of preactivated Al-TiCl4 catalyst.
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 5 (1967), S. 1037-1038 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 215-226 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The influence of preparative conditions on the molecular weight and stereoregularity distributions of polypropylene was investigated. The stereoregularity distribution is narrowed by using a highly stereospecific catalyst, by decreasing the polymerization temperature, and for the three-component catalyst by keeping the mole proportion of the electron-donating third component at 0.5. The molecular weight distribution can be narrowed by using a highly stereospecific catalyst, a high monomer concentration, and a high polymerization temperature, and by having a lower conversion, particularly at low monomer concentration. The possibility of long-chain branching in polypropylene was indicated by data from the fractionation of tritium-labeled polymers.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 2135-2147 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The chemistry of three-component coordination catalysts for the polymerization of α-olefins is very complex. The present investigation was initiated to elucidate the chemistry involved in the interaction of third-component compounds such as hexamethylphosphoric triamide, tributylamine, triphenylphosphine, or dimethylformamide with ethylaluminum dichloride. The present chemical and spectral data demonstrate that ethylaluminum dichloride and third-component compounds form stable complexes even at temperatures up to 100°C. in the absence of solvents or in homogeneous solutions. These data are in agreement with the fact that organoaluminum compounds form stable complexes with a variety of electron-donor compounds. The ethylaluminum dichloride third-component complexes in combination with titanium(III) chloride produce highly stereospecific catalysts for the polymerization of α-olefins.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 2407-2424 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is well known that mixtures of alkylaluminum dihalides and transition metal halides, such as titanium(III) chloride, are ineffective as catalysts for the stereospecific polymerization of α-olefins. It has been discovered that the addition of a third compound, derived from one or more of the strongly complexing ligand elements such as nitrogen oxygen, and phosphorus, to such mixtures leads to catalysts having the highest stereospecificities known. In the present work, studies were made of the effect of various third components on the activity and stereospecificity of these catalysts in the polymerization of propylene. The stereospecificity and activity of three-component catalysts of this type were dependent upon the ratio of the third component to the alkyaluminum dihalide. Optimum stereospecificity and activity were usually obtained at ratios in the range of 0.5-0.7. In general, catalytic activity increased with increasing basicity of the third component. Both stereospecificity and activity were influenced by the nature of the halogen atoms in the alkylaluminum dihalide, whereas the nature of the alkyl group affected only the activity, with the ethyl group providing the most active catalysts. The most stereospecific catalyst was made from a mixture of ethylaluminum diiodide, hexamethylphosphoric triamide, and violet titanium(III) chloride.
    Additional Material: 7 Ill.
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  • 7
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The active-site concentration was determined by using tritium labeling on three coordinate anionic catalysts containing violet titanium(III) chloride [hereafter referred to as titanium(III) chloride or TiCl3]. These catalysts were used in the polymerization of propylene. Three-component catalysts, as well as two-component catalysts, were investigated. Previous estimates of active-site concentrations for (C2H5)2AlCl - TiCl3 catalysts appear to be too high by at least a factor of 10. The reason for the previous high estimates can be attributed to the marked reduction in chain-transfer rate which occurs when the amount of polymer formed exceeds about 2 g./g. TiCl3. The chain-transfer process appears to involve both alkylaluminum and monomer, but the effective monomer concentration is apparently not reduced until a later stage in the polymerization. The propagation rate is, therefore, unaffected; but the transfer rate is reduced, leading to the formation of polymer with much higher molecular weight. Extension of this process could lead to the observed broad distribution of molecular weights in polypropylene. As a result of the low value of active-site concentrations [about 10-3 mole/mole titanium(III) chloride], the absolute value calculated for the propagation rate constant for propylene polymerization is in the range of 50 l./mole sec., and the average lifetime of a growing polymer molecule during the early stages of the polymerization is about 1 min.
    Additional Material: 7 Ill.
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  • 8
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymerization of propylene and 1-butene with highly stereospecific three-component coordination catalysts produced multiblock crystalline copolymers having stereo-regular sequences of both propylene and 1-butene. Copolymers containing from 3 to about 80% 1-butene had two DTA melting points which were attributable to polypropylene and poly-1-butene crystallinity. Those containing from 18 to about 70% 1-butene had x-ray diffraction patterns showing peaks characteristic of polypropylene and form I poly-1-butene, but form II poly-1-butene crystallinity was never observed. The multiblock copolymer structure observed is also supported by the fact that the product of the reactivity ratios is greater than unity. The composition distributions of low-conversion and continuously prepared copolymers were similar and relatively broad. For example, copolymers containing an average of 12% 1-butene had species containing from 5-30% 1-butene. High-conversion copolymers had an even broader composition distribution due to the gradual increase of the 1-butene concentration in the comonomer mixture as the copolymerization proceeded. The absence of homopolymers was demonstrated by fractionation. The ability to detect homopolymers was proved by the fact that a mixture of stereoregular polypropylene and poly-1-butene were readily separated. Increasing the amount of 1-butene tended to decrease those properties dependent upon crystallinity such as hardness, tensile strength, stiffness, density, and melting point, but tended to improve significantly the impact strength, low temperature properties, and clarity of molded objects. These duocrystalline copolymers retained a much higher level of properties than that observed for random copolymers prepared with less stereospecific coordination catalysts.
    Additional Material: 8 Ill.
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